Song G G, Lee Y H
Division of Rheumatology, Department of Internal Medicine, Korea University College of Medicine, Seoul, Korea.
Division of Rheumatology, Department of Internal Medicine, Korea University College of Medicine, Seoul, Korea
Genet Mol Res. 2014 Oct 7;13(4):8174-83. doi: 10.4238/2014.October.7.12.
The purpose of this study was to examine whether the insertion (I) or deletion (D) polymorphism of the angiotensin-converting enzyme gene (ACE) is associated with susceptibility to systemic sclerosis (SSc). A meta-analysis examining the associations between the ACE I/D polymorphism and SSc was conducted in overall and European populations using 1) allelic contrast (D vs I); 2) recessive (DD vs ID + II); 3) dominant (DD + ID vs II); and 4) additive (DD vs ID vs II) models. A total of 7 studies consisting of 837 cases and 754 controls were available for meta-analysis. The meta-analysis revealed no association between the D allele and SSc in any study subjects [odds ratio (OR) = 0.956, 95% confidence interval (CI) = 0.733-1.246, P = 0.737]. Stratification by ethnicity indicated no association between the D allele of the ACE I/D polymorphism and SSc in Europeans (OR = 1.117, 95%CI = 0.776-1.607, P = 0.551). Meta-analysis using all other genetic models showed the same D allele pattern in the overall and European groups. This meta-analysis showed that the ACE I/D polymorphism was not associated with susceptibility to SSc in the study subjects and in Europeans.
本研究的目的是检验血管紧张素转换酶基因(ACE)的插入(I)或缺失(D)多态性是否与系统性硬化症(SSc)的易感性相关。我们使用1)等位基因对比(D vs I);2)隐性(DD vs ID + II);3)显性(DD + ID vs II);以及4)加性(DD vs ID vs II)模型,在总体人群和欧洲人群中进行了一项荟萃分析,以研究ACE I/D多态性与SSc之间的关联。共有7项研究,包括837例病例和754例对照可用于荟萃分析。荟萃分析显示,在任何研究对象中,D等位基因与SSc之间均无关联[比值比(OR)= 0.956,95%置信区间(CI)= 0.733 - 1.246,P = 0.737]。按种族分层表明,在欧洲人中,ACE I/D多态性的D等位基因与SSc之间无关联(OR = 1.117,95%CI = 0.776 - 1.607,P = 0.551)。使用所有其他遗传模型进行的荟萃分析在总体人群和欧洲人群组中显示出相同的D等位基因模式。这项荟萃分析表明,在研究对象和欧洲人中,ACE I/D多态性与SSc的易感性无关。